SHOCKING: FDA Delays Moderna Vaccine For Adolescents Due To Myocarditis Risk In Children!
Sweden and Denmark were the first countries to announce that they stopped the Moderna COVID-19 vaccine for people under the age of 30 because it may cause dangerous side effects, including myocarditis.
It’s breaking news.
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Two nations saw that the vaccine’s side effects were horrible enough to ban its application.
Pfizer filed for FDA approval of the vaccine for children at the age of 5 to 11.
The VAERS tracking website shows that 4,144 people have died in the US due to the Moderna C-19 vaccine and 11,346 due to the Pfizer vaccine.
This Monday, the FDA delayed the approval for the Moderna vaccine in children.
The Examiner covered this story:
The U.S. Food and Drug Administration announced Friday it would delay its decision on administration of the Moderna vaccine to adolescents, citing concerns the shot may lead to a heightened risk of a rare heart condition.
The FDA has not yet determined if the risk is higher for adolescents, but the agency is planning to review the data further before extending the vaccine’s eligibility, according to the Wall Street Journal.
“I think people can be reassured that the risk of myocarditis with an mRNA vaccine is low, it appears to be balanced between the different products,” Paul Burton, Moderna’s chief medical officer, told the outlet.
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